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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
The antibody detects endogenous levels of total TSPEAR protein.
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012].
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: protein TSPEAR; Thrombospondin-type laminin G domain and EAR repeat-containing protein; thrombospondin-type laminin G domain and EAR repeats-containing protein; TSP-EAR
基因别名: C21orf29; DFNB98; ECTD14; STHAG10; TSP-EAR; TSPEAR
UniProt ID: (Human) Q8WU66
Entrez Gene ID: (Human) 54084